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Showing results 41 to 60 of 69
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TypeAuthor(s)TitleOther TitlesCitationCitation(alt)Issue Date
article (author version)Yabe, Ichiro; Soma, Hiroyuki; Takei, Asako; Fujiki, Naoto; Yanagihara, Tetsuro; Sasaki, HidenaoMSA-C is the predominant clinical phenotype of MSA in Japan : Analysis of 142 patients with probable MSA-Journal of the Neurological Sciences-15-Nov-2006
articleMatsushima, Masaaki; Yabe, Ichiro; Sakushima, Ken; Kanatani, Yasuhiro; Nishimoto, Naoki; Matsuoka, Takeshi; Sawada, Jun; Uesugi, Haruo; Sako, Kazuya; Takei, Asako; Tamakoshi, Akiko; Shimohama, Shun; Sato, Norihiro; Kikuchi, Seiji; Sasaki, HidenaoMultiple system atrophy in Hokkaido, Japan : a prospective registry study of natural history and symptom assessment scales followed for 5 years.-BMJ open-Dec-2020
articleYabe, Ichiro; Yaguchi, Hiroaki; Kato, Yasutaka; Miki, Yasuo; Takahashi, Hidehisa; Tanikawa, Satoshi; Shirai, Shinichi; Takahashi, Ikuko; Kimura, Mari; Hama, Yuka; Matsushima, Masaaki; Fujioka, Shinsuke; Kano, Takahiro; Watanabe, Masashi; Nakagawa, Shin; Kunieda, Yasuyuki; Ikeda, Yoshio; Hasegawa, Masato; Nishihara, Hiroshi; Ohtsuka, Toshihisa; Tanaka, Shinya; Tsuboi, Yoshio; Hatakeyama, Shigetsugu; Wakabayashi, Koichi; Sasaki, HidenaoMutations in bassoon in individuals with familial and sporadic progressive supranuclear palsy-like syndrome-Scientific Reports-16-Jan-2018
article (author version)Sakushima, Ken; Tsuboi, Satoshi; Yabe, Ichiro; Hida, Kazutoshi; Terae, Satoshi; Uehara, Ritei; Nakano, Imaharu; Sasaki, HidenaoNationwide survey on the epidemiology of syringomyelia in Japan-Journal of the Neurological Sciences-15-Feb-2012
article (author version)Shirai, Shinichi; Mito, Yasunori; Nojo, Tatsuru; Yaguchi, Hiroaki; Takahashi, Toshiyuki; Sato, Kazunori; Hirotani, Makoto; Kano, Takahiro; Yabe, Ichiro; Sasaki, HidenaoNeuromyelitis optica spectrum disorders accompanying subarachnoid hemorrhage and reversible white matter lesions-Neurology and Clinical Neuroscience-Jan-2014
article (author version)Yabe, Ichiro; Tanino, Mishie; Yaguchi, Hiroaki; Takiyama, Akihiro; Cai, Huaying; Kanno, Hiromi; Takahashi, Ikuko; Hayashi, Yukiko K.; Watanabe, Masashi; Takahashi, Hidehisa; Hatakeyama, Shigetsugu; Tanaka, Shinya; Sasaki, HidenaoPathology of frontotemporal dementia with limb girdle muscular dystrophy caused by a DNAJB6 mutation-Clinical neurology and neurosurgery-Dec-2014
articleNomura, Taichi; Iwata, Ikuko; Naganuma, Ryoji; Matsushima, Masaaki; Satoh, Katsuya; Kitamoto, Tetsuyuki; Yabe, IchiroA patient with spastic paralysis finally diagnosed as V180I genetic Creutzfeldt-Jakob disease 9 years after onset-Prion-1-Jan-2020
articleMatsushima, Masaaki; Tarisawa, Monami; Nomura, Taichi; Oshima, Yuki; Yoshino, Masanao; Shibata, Yuka; Wakita, Masahiro; Shirai, Shinichi; Iwata, Ikuko; Yaguchi, Hiroaki; Yabe, IchiroPractice of Hereditary ATTR Amyloidosis in Non-endemic Areas of Japan-Internal Medicine-1-Jun-2023
article (author version)Iwami, Kosuke; Nakamichi, Kazuo; Matsushima, Masaaki; Nagai, Azusa; Shirai, Shinichi; Nakakubo, Sho; Takahashi-Iwata, Ikuko; Yamada, Masafumi; Yabe, IchiroProgressive multifocal leukoencephalopathy with mild clinical conditions and detection of archetype-like JC virus in cerebrospinal fluid-Journal of Neurovirology-1-Dec-2021
article (author version)Shibata, Yuka; Matsushima, Masaaki; Yabe, Ichiro; Matsuda, Koichiro; Nagai, Azusa; Kano, Takahiro; Yamada, Takahiro; Sekijima, Yoshiki; Sasaki, HidenaoPseudo-homozygous mutation due to a primer site polymorphism in hereditary ATTR amyloidosis : a pitfall of PCR-based genetic testing-Amyloid-2017
article (author version)Uwatoko, Hisashi; Yabe, Ichiro; Shirai, Shinichi; Takahashi, Ikuko; Matsushima, Masaaki; Kano, Takahiro; Sasaki, HidenaoPseudodystonia in sarcoid myopathyPseudo-dystonia in sarcoid myopathyNeurology and Clinical Neuroscience-Jan-2017
article (author version)Shirai, Shinichi; Yabe, Ichiro; Matsushima, Masaaki; Ito, Yoichi M.; Yoneyama, Mitsuru; Sasaki, HidenaoQuantitative evaluation of gait ataxia by accelerometers-Journal of the Neurological Sciences-15-Nov-2015
article (author version)Yabe, Ichiro; Matsushima, Masaaki; Yoshida, Kunihiro; Ishikawa, Kinya; Shirai, Shinichi; Takahashi, Ikuko; Sasaki, HidenaoRare frequency of downbeat positioning nystagmus in spinocerebellar ataxia type 31-Journal of the Neurological Sciences-15-Mar-2015
article (author version)Matsushima, Masaaki; Yabe, Ichiro; Uwatoko, Hisashi; Shirai, Sinichi; Hirotani, Makoto; Sasaki, HidenaoReliability of the Japanese version of the Berg balance scale.-Internal medicine-2014
article (author version)Matsushima, Masaaki; Yabe, Ichiro; Hirotani, Makoto; Kano, Takahiro; Sasaki, HidenaoReliability of the Japanese version of the scales for outcomes in Parkinson's disease-autonomic questionnaire.-Clinical neurology and neurosurgery-Sep-2014
article (author version)Shirai, Shinichi; Yabe, Ichiro; Takahashi-Iwata, Ikuko; Matsushima, Masaaki; Ito, Yoichi M.; Takakusaki, Kaoru; Sasaki, HidenaoThe Responsiveness of Triaxial Accelerometer Measurement of Gait Ataxia Is Higher than That of the Scale for the Assessment and Rating of Ataxia in the Early Stages of Spinocerebellar Degeneration-Cerebellum-Aug-2019
articleYoshii, Kentaro; Takahashi-Iwata, Ikuko; Shirai, Shinichi; Kobayashi, Shintaro; Yabe, Ichiro; Sasaki, HidenaoA Retrospective Epidemiological Study of Tick-Borne Encephalitis Virus in Patients with Neurological Disorders in Hokkaido, Japan-Microorganisms-Nov-2020
article (author version)Eguchi, Katsuki; Tsuzaka, Kazufumi; Yabe, Ichiro; Sasaki, HidenaoReversible splenial lesion in new-onset refractory status epilepticus : A case report-Clinical neurology and neurosurgery-Aug-2019
article (author version)Yaguchi, Hiroaki; Takahashi, Ikuko; Tashiro, Jun; Tsuji, Sachiko; Yabe, Ichiro; Sasaki, HidenaoScapular Winging as a Symptom of Cervical Flexion Myelopathy-Internal Medicine-17-Apr-2007
article (author version)Basri, Rehana; Yabe, Ichiro; Soma, Hiroyuki; Sasaki, HidenaoSpectrum and prevalence of autosomal dominant spinocerebellar ataxia in Hokkaido, the northern island of Japan : a study of 113 Japanese families-Journal of Human Genetics-Oct-2007
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